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Acupuncture Versus Clonazepam in Burning Mouth Syndrome (ACUCLONBMS)

Primary Purpose

Burning Mouth Syndrome

Status
Completed
Phase
Early Phase 1
Locations
Study Type
Interventional
Intervention
Clonazepam
acupuncture
Sponsored by
University of Zagreb
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Burning Mouth Syndrome

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

Clinical diagnosis of burning mouth syndrome Clinically normal appearance of oral mucosa Must be able to swallow tablets

Exclusion Criteria:

Oral mucosal lesions Anemia

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Active Comparator

    Experimental

    Arm Label

    clonazepam

    acupuncture

    Arm Description

    Twenty two patients took clonazepam two times a day (0.5 mg) in the morning and after two weeks one tablet (0.5 mg) in the morning and another tablet (0.5 mg) in the evening during the next two weeks.

    Traditional Chinese acupuncture was performed on 20 participants 3 times during one week for four weeks. Intervention was performed on acupuncture points as follows: the points ST 8 (stomach- tou wei), GB 2, TE 21, SI 19 (small intestine- ting gong), SI 18 (small intestine- quan liao), LI 4 (large intestine-Yuan) on both sides of the body as well as GV 20 (Governing vessel-bai hui). Each session lasted half an hour. Sterile acupuncture needles made from surgical stainless steel silicone coated with spring handle were used. The dimensions of the chosen needles were 0.25 in diameter and 30 mm length, inserted at the depth of the 0.5-1 cm. The elicited response was of the type "de qi" accompanied by redness and a feeling of numbness around the needles.

    Outcomes

    Primary Outcome Measures

    Pain intensity
    Pain intensity measured by the visual analogue scale

    Secondary Outcome Measures

    The Leeds Assessment of Neuropathic Symptoms and Signs (LANSS) Pain Scale
    Assessment of neuropathic pain measured by validated instrument (LANSS pain scale)
    Cognitive function
    Assesment of cognitive function measured by validated instrument ( MoCA cognitive test)
    Depression
    Assesment of depressive symptoms by use of validated instrument (Beck Depression Inventory)
    Quality of life
    Assesment of quality of life by validated instrument (Short Forma Health Survey: SF-36)

    Full Information

    First Posted
    February 13, 2015
    Last Updated
    March 2, 2015
    Sponsor
    University of Zagreb
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02382029
    Brief Title
    Acupuncture Versus Clonazepam in Burning Mouth Syndrome
    Acronym
    ACUCLONBMS
    Official Title
    The Effectiveness of Acupuncture Versus Clonazepam in the Patients With Burning Mouth Syndrome
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    March 2015
    Overall Recruitment Status
    Completed
    Study Start Date
    March 2014 (undefined)
    Primary Completion Date
    November 2014 (Actual)
    Study Completion Date
    November 2014 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    University of Zagreb

    4. Oversight

    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    Objective: Burning mouth syndrome (BMS) is chronic oral condition characterized with burning symptoms which affects perimenopausal and postmenopausal women. It seems that neuropathy might be the underlying cause of the condition. There are still insufficient data regarding successful therapy. The aim of this study was to compare efficacy of acupuncture and clonazepam in 42 BMS patients (38 women, 4 men), age range 66.7±12 years. Methods: Patients were randomly divided into two groups. Acupuncture was performed in group I during four weeks, 3 times per week on the points ST 8, GB 2, TB 21, SI 19, SI 18, LI 4 on both sides of the body as well as GV 20, each session lasted half an hour.Group II patients took clonazepam two times a day (0.5 mg) in the morning and after two weeks two tablets (0.5 mg) in the morning and in the evening during the next two weeks. Prior to and one month after either therapy, participants fulfilled questionnaires: visual analogue scale, Beck depression inventory, LANSS pain scale, 36-item short form Health Survey (SF-36) and Montreal Cognitive Assessment (MoCA). Statistical analysis was performed by use of Student t test and Pearson's correlation test. P values lower than 0.05 were considered significant.
    Detailed Description
    This study was approved by Ethical Committee of the School of dentistry in Zagreb. Prior to the study every participant signed informed consent according to the Helsinki II. All patient were recruited from the Department of Oral medicine, School of dentistry in Zagreb. Patients were randomized by simple randomization method- flipping a coin (heads - acupuncture, tails - clonazepam). Inclusion criteria were symptoms of burning in the oral cavity with clinically healthy appearance of the oral mucosa. Burning symptoms were continuous throughout the day and lasted for more than 6 months. Some of the patients also had hyposalivation and disturbed taste. Prior to the either therapy as well as after the therapy (one month after the therapy has finished) every participant fulfilled following questionnaires: visual analogue scale (VAS) which referred to the severity of burning symptoms, Beck depression inventory (BDI), The Leeds assessment of neuropathic symptoms and signs (LANSS) Pain Scale, 36-item short form Health Survey (SF-36) total sum score and Montreal Cognitive Assessment (MoCA). Arm (I) traditional Chinese acupuncture - performed 3 times during one week for four weeks on the points ST 8 (stomach- tou wei), GB 2, TE 21, SI 19 (small intestine- ting gong), SI 18 (small intestine- quan liao), LI 4 (large intestine-Yuan) on both sides of the body as well as GV 20 (Governing vessel-bai hui) and each session lasted half an hour. We used sterile acupuncture needles from surgical stainless steel silicone coated with spring handle, the dimensiones of the chosen needles were 0.25 in diameter and 30 mm lenght, inserted at the depht of the 0.5-1 cun. The elicited response was of the type "de qi" accompanied by redness and a feeling of numbness around the needles. Arm (II) Clonazepam - patients took clonazepam two times a day (0.5 mg) in the morning and after two weeks one tablet (0.5 mg) in the morning and another tablet (0.5 mg) in the evening during the next two weeks. Statistical analysis was performed by use of Student t test and Pearson's correlation test. P values lower than 0.05 were considered significant.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Burning Mouth Syndrome

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Early Phase 1
    Interventional Study Model
    Parallel Assignment
    Masking
    Investigator
    Allocation
    Randomized
    Enrollment
    4 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    clonazepam
    Arm Type
    Active Comparator
    Arm Description
    Twenty two patients took clonazepam two times a day (0.5 mg) in the morning and after two weeks one tablet (0.5 mg) in the morning and another tablet (0.5 mg) in the evening during the next two weeks.
    Arm Title
    acupuncture
    Arm Type
    Experimental
    Arm Description
    Traditional Chinese acupuncture was performed on 20 participants 3 times during one week for four weeks. Intervention was performed on acupuncture points as follows: the points ST 8 (stomach- tou wei), GB 2, TE 21, SI 19 (small intestine- ting gong), SI 18 (small intestine- quan liao), LI 4 (large intestine-Yuan) on both sides of the body as well as GV 20 (Governing vessel-bai hui). Each session lasted half an hour. Sterile acupuncture needles made from surgical stainless steel silicone coated with spring handle were used. The dimensions of the chosen needles were 0.25 in diameter and 30 mm length, inserted at the depth of the 0.5-1 cm. The elicited response was of the type "de qi" accompanied by redness and a feeling of numbness around the needles.
    Intervention Type
    Drug
    Intervention Name(s)
    Clonazepam
    Other Intervention Name(s)
    Rivotril
    Intervention Description
    Active medical treatment for burning mouth syndrome
    Intervention Type
    Other
    Intervention Name(s)
    acupuncture
    Intervention Description
    Traditional chinese acupuncture
    Primary Outcome Measure Information:
    Title
    Pain intensity
    Description
    Pain intensity measured by the visual analogue scale
    Time Frame
    6 months
    Secondary Outcome Measure Information:
    Title
    The Leeds Assessment of Neuropathic Symptoms and Signs (LANSS) Pain Scale
    Description
    Assessment of neuropathic pain measured by validated instrument (LANSS pain scale)
    Time Frame
    6 months
    Title
    Cognitive function
    Description
    Assesment of cognitive function measured by validated instrument ( MoCA cognitive test)
    Time Frame
    6 months
    Title
    Depression
    Description
    Assesment of depressive symptoms by use of validated instrument (Beck Depression Inventory)
    Time Frame
    6 months
    Title
    Quality of life
    Description
    Assesment of quality of life by validated instrument (Short Forma Health Survey: SF-36)
    Time Frame
    6 months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Clinical diagnosis of burning mouth syndrome Clinically normal appearance of oral mucosa Must be able to swallow tablets Exclusion Criteria: Oral mucosal lesions Anemia

    12. IPD Sharing Statement

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    Acupuncture Versus Clonazepam in Burning Mouth Syndrome

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